Canonical Allele Identifier: CA915944783

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 817319
• ClinVar RCV Id: RCV001008439
• dbSNP Id: rs1583479817

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189750dup , CM000668.2:g.157189750dup	GRCh38
NC_000006.11:g.157510884dup , CM000668.1:g.157510884dup	GRCh37
NC_000006.10:g.157552576dup	NCBI36
NG_032093.1:g.416821dup
NG_032093.2:g.416821dup
NG_066624.1:g.418725dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3869dup	ENSP00000055163.8:p.His1290GlnfsTer26
ENST00000414678.8:c.3938dup	ENSP00000412835.3:p.His1313GlnfsTer26
ENST00000637015.2:c.4157dup	ENSP00000489729.2:p.His1386GlnfsTer26
ENST00000346085.10:c.3908dup	ENSP00000344546.5:p.His1303GlnfsTer26
ENST00000350026.10:c.3620dup	ENSP00000055163.7:p.His1207GlnfsTer26
ENST00000414678.7:c.2186dup	ENSP00000412835.2:p.His729GlnfsTer26
ENST00000635849.1:c.1349dup	ENSP00000490948.1:p.His450GlnfsTer26
ENST00000635957.1:c.983dup	ENSP00000490385.1:p.His328GlnfsTer25
ENST00000636930.2:c.4028dup MANE Select	ENSP00000490491.2:p.His1343GlnfsTer26
ENST00000636940.1:n.2025dup
ENST00000637015.1:c.1396dup
ENST00000637568.1:c.1310dup
ENST00000637741.1:n.694dup
ENST00000637810.1:c.1370dup	ENSP00000489636.1:p.His457GlnfsTer26
ENST00000637904.1:c.1529dup	ENSP00000490550.1:p.His510GlnfsTer26
ENST00000647938.1:c.3659dup	ENSP00000498155.1:p.His1220GlnfsTer26
ENST00000346085.9:c.3659dup	ENSP00000344546.4:p.His1220GlnfsTer26
ENST00000350026.9:c.3620dup	ENSP00000055163.7:p.His1207GlnfsTer26
ENST00000414678.6:c.2186dup	ENSP00000412835.2:p.His729GlnfsTer26
NM_017519.2:c.3620dup	NP_059989.2:p.His1207GlnfsTer26
NM_020732.3:c.3659dup	NP_065783.3:p.His1220GlnfsTer26
XM_005267069.3:c.3779dup	XP_005267126.2:p.His1260GlnfsTer26
XM_011535984.1:c.2858dup	XP_011534286.1:p.His953GlnfsTer26
XM_011535985.1:c.2678dup	XP_011534287.1:p.His893GlnfsTer26
XM_011535986.1:c.2438dup	XP_011534288.1:p.His813GlnfsTer26
XM_011535987.1:c.2057dup	XP_011534289.1:p.His686GlnfsTer26
XM_011535988.1:c.920dup	XP_011534290.1:p.His307GlnfsTer26
NM_001346813.1:c.3779dup	NP_001333742.1:p.His1260GlnfsTer26
NM_001363725.1:c.1529dup	NP_001350654.1:p.His510GlnfsTer26
XM_011535984.2:c.3989dup	XP_011534286.2:p.His1330GlnfsTer26
XM_011535988.3:c.920dup	XP_011534290.1:p.His307GlnfsTer26
XM_017011103.2:c.3890dup	XP_016866592.1:p.His1297GlnfsTer26
XM_017011104.1:c.3860dup	XP_016866593.1:p.His1287GlnfsTer26
XM_017011105.2:c.3830dup	XP_016866594.1:p.His1277GlnfsTer26
XM_017011106.2:c.3701dup	XP_016866595.1:p.His1234GlnfsTer26
XM_017011107.2:c.3680dup	XP_016866596.1:p.His1227GlnfsTer26
XR_002956289.1:n.4072dup
NM_001363725.2:c.1529dup	NP_001350654.1:p.His510GlnfsTer26
NM_001371656.1:c.3908dup	NP_001358585.1:p.His1303GlnfsTer26
NM_001374820.1:c.3908dup	NP_001361749.1:p.His1303GlnfsTer26
NM_001374828.1:c.4028dup MANE Select	NP_001361757.1:p.His1343GlnfsTer26
NM_017519.3:c.3869dup	NP_059989.3:p.His1290GlnfsTer26